Canonical Allele Identifier: CA2608894070
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077062T>A , CM000672.2:g.43077062T>A GRCh38
NC_000010.10:g.43572510T>A , CM000672.1:g.43572510T>A GRCh37
NC_000010.9:g.42892516T>A NCBI36
NG_007489.1:g.4994T>A , LRG_518:g.4994T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-197T>A ENSP00000347942.3:n.-197T>A
XM_011540027.1:c.-197T>A XP_011538329.1:n.-197T>A
NM_020630.5:c.-197T>A NP_065681.1:n.-197T>A
NM_020975.5:c.-197T>A NP_066124.1:n.-197T>A